A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3587046



Internal ID7058428
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:30067657..30068741hg38UCSC Ensembl
Innerchr19:30558564..30559648hg19UCSC Ensembl
Innerchr19:35250404..35251488hg18UCSC Ensembl
Cytoband19q12
Allele length
AssemblyAllele length
hg381085
hg191085
hg181085
Variant TypeCNV loss
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv999868
Supporting Variants
SamplesHuRef
Known Genes
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3587046
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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